Canonical Allele Identifier: CA237810677

Gene: ARHGEF25

Linked Data

• dbSNP Id: rs762759558
• gnomAD v4: 12-57614243-A-G
• MyVariant Identifiers: chr12:g.58008026A>G (hg19) ; chr12:g.57614243A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57614243A>G , CM000674.2:g.57614243A>G	GRCh38
NC_000012.11:g.58008026A>G , CM000674.1:g.58008026A>G	GRCh37
NC_000012.10:g.56294293A>G	NCBI36
NG_053182.1:g.9064A>G
NG_053182.2:g.9128A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286494.9:c.657-88A>G MANE Select	ENSP00000286494.4:n.657-88A>G
ENST00000286494.8:c.657-88A>G	ENSP00000286494.4:n.657-88A>G
ENST00000333972.11:c.774-88A>G	ENSP00000335560.7:n.774-88A>G
ENST00000471370.5:n.250A>G
ENST00000616622.1:c.339-88A>G	ENSP00000484303.1:n.339-88A>G
NM_001111270.2:c.774-88A>G	NP_001104740.1:n.774-88A>G
NM_182947.3:c.657-88A>G	NP_891992.2:n.657-88A>G
NR_046223.1:n.1147-88A>G
NM_001347933.1:c.657-88A>G	NP_001334862.1:n.657-88A>G
NM_182947.4:c.657-88A>G MANE Select	NP_891992.3:n.657-88A>G
NM_001111270.3:c.774-88A>G	NP_001104740.2:n.774-88A>G
NM_001347933.2:c.657-88A>G	NP_001334862.2:n.657-88A>G
NR_046223.2:n.1147-88A>G